| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110689630-110689881 | Rare:40 | ||||
| chr12:110689952-110690112 | Rare:27 | ||||
| chr12:110742760-110743258 | Common:3; Rare:163 | ||||
| chr12:110913332-110913817 | Common:4; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:111368984-111369269 | Common:1; Rare:75 | ||||
| chr12:111405310-111405511 | Common:1; Rare:36 | ||||
| chr12:111405738-111406052 | Rare:99 | ||||
| chr12:111434847-111434912 | Common:1; Rare:17 | ||||
| chr12:111434970-111435041 | Rare:16 | ||||
| chr12:111435048-111435255 | Rare:47 | ||||
| chr12:111597400-111597465 | Rare:9 | ||||
| chr12:111598918-111598964 | Common:2; Rare:31 | ||||
| chr12:111599232-111599723 | Common:4; Rare:168 | ||||
| chr12:111599725-111599940 | Rare:45 | ||||
| chr12:111600073-111600121 | Rare:13 |